Growth and Etching of Centimeter-Scale Self-Assembly Graphene–h-BN Super-Ordered Arrays: Implications for Integrated Electronic Devices

2022 ◽  
Author(s):  
Menghan Li ◽  
Yajing Sun ◽  
Xiao Xue ◽  
Xueying Lu ◽  
Zilong Guo ◽  
...  
Keyword(s):  
Self Assembly ◽  
Electronic Devices ◽  
Ordered Arrays

Chiral Molecular Cavities of Calix[4]Crown on Au(111)

2008 ◽  
Vol 8 (11) ◽  
pp. 5702-5707 ◽  
Author(s):  
Ge-Bo Pan ◽  
Jun Luo ◽  
Qi-Yu Zheng ◽  
Li-Jun Wan
Keyword(s):  
Self Assembly ◽  
Chiral Recognition ◽  
Scanning Tunneling ◽  
Racemic Mixture ◽  
Tunneling Microscopy ◽  
Geometrical Structures ◽  
Simple Method ◽  
Ordered Structures ◽  
Ordered Arrays ◽  
Stm Images

Well-ordered arrays of chiral molecular cavities have been constructed by self-assembly of inherently chiral calix[4]crown on Au(111) in 0.1 M HClO4 solution and investigated by scanning tunneling microscopy (STM). The chiral features are clearly observed in high resolution STM images. It is found that the adsorption of the two enantiomers results in the same ordered structures with upright orientation on Au(111). Moreover, only phase separation has been observed for the racemic mixture of the two enantiomers in the experiment. This is mainly due to the weak molecule-substrate interaction as well as asymmetric geometrical structures of the two enantiomers. The present study provides a simple method for construction of ordered arrays of chiral molecular cavities, which are of potential in chemical sensors, chiral recognition, and nonlinear optics.

scholarly journals Nanostructural self-assembly of iridescent feather barbules through depletion attraction of melanosomes during keratinization

2011 ◽  
Vol 9 (69) ◽  
pp. 734-743 ◽  
Author(s):  
Rafael Maia ◽  
Regina H. F. Macedo ◽  
Matthew D. Shawkey
Keyword(s):  
Self Assembly ◽  
Light And Electron Microscopy ◽  
Single Layer ◽  
Metabolic Cost ◽  
Condition Dependence ◽  
Developmental Pathway ◽  
Ordered Arrays ◽  
Cellular Control ◽  
Ornamental Traits ◽  
Nanostructural Organization

Avian plumage colours are model traits in understanding the evolution of sexually selected ornamental traits. Paradoxically, iridescent structural colours, probably the most dazzling of these traits, remain the most poorly understood. Though some data suggest that expression of bright iridescent plumage colours produced by highly ordered arrays of melanosomes and keratin is condition-dependent, almost nothing is known of their ontogeny and thus of any developmental mechanisms that may be susceptible to perturbation. Here, we use light and electron microscopy to compare the ontogeny of iridescent male and non-iridescent female feathers in blue-black grassquits. Feather barbules of males contain a single layer of melanosomes bounded by a thin layer of keratin-producing blue iridescent colour, while those of females contain disorganized melanosomes and no outer layer. We found that nanostructural organization of male barbules occurs late in development, following death of the barbule cell, and is thus unlikely to be under direct cellular control, contrary to previous suggestions. Rather, organization appears to be caused by entropically driven self-assembly through depletion attraction forces that pin melanosomes to the edge of barbule cells and to one another. These forces are probably stronger in developing barbules of males than of females because their melanosomes are (i) larger, (ii) more densely packed, and (iii) more homogeneously distributed owing to the more consistent shape of barbules during keratinization. These data provide the first proposed developmental pathway for iridescent plumage colours, and suggest that any condition dependence of iridescent barbules is likely driven by factors other than direct metabolic cost.

scholarly journals Pyramidal Heteroanion-Directed and Reduced MoV-Driven Assembly of Multi-Layered Polyoxometalate Cages

2018 ◽  
Author(s):  
Qi Zheng, ◽  
Manuel Kupper ◽  
Weimin Xuan ◽  
Hirofumi Oki ◽  
Ryo Tsunashima ◽  
...  
Keyword(s):  
Self Assembly ◽  
Electronic Materials ◽  
Electronic Devices ◽  
Mixed Valence ◽  
The Self ◽  
Model Structure ◽  
Redox Titration ◽  
Metal Centers ◽  
Redox Active ◽  
Tetrabutyl Ammonium

The fabrication of redox-active polyoxometalates (POMs) that can switch between multiple states is critical for their application in electronic devices, yet, a sophisticated synthetic methodology is not well developed for such cluster types. Here we describe the heteroanion-directed and reduction-driven assembly of a series of multi-layered POM cages 1-10 templated by 1-3 redox-active pyramidal heteroanions. The heteroanions greatly affect the selfassembly of the resultant POM cages, leading to the generation of unprecedented three-layered peanut-shaped - 4, 7 and 8 - or bulletshaped - 5 and 6 - structures. The introduction of reduced molybdate is essential for the self-assembly of the compounds and results in mixed-metal (W/Mo), and mixed-valence (WVI/MoV) 1-10, as confirmed by redox titration, UV-Vis-NIR, NMR spectroscopy and mass spectrometry. 11, the tetrabutyl ammonium (TBA) salt derivative of the fully oxidized 3, is produced as a model structure for measurements to confirm that 1-10 are a statistical mixture of isostructural clusters with different ratios of W/Mo. Finally, multilayered POM cages exhibit dipole relaxations due to the presence of mixed valence WVI/MoV metal centers, demonstrating their potential uses for electronic materials.

scholarly journals Bottom-up device fabrication via the seeded growth of polymer-based nanowires

2020 ◽  
Vol 11 (24) ◽  
pp. 6222-6228
Author(s):  
Osama El-Zubir ◽  
Emily L. Kynaston ◽  
Jessica Gwyther ◽  
Ali Nazemi ◽  
Oliver E. C. Gould ◽  
...  
Keyword(s):  
Self Assembly ◽  
Electronic Devices ◽  
Device Fabrication ◽  
Seeded Growth ◽  
Bottom Up

Living crystallisation-driven self-assembly facilitates the bottom-up assembly of electronic devices.

scholarly journals Redox Active Ordered Arrays via Metal Initiated Self-Assembly of Terpyridine Based Ligands†

2001 ◽  
Vol 105 (37) ◽  
pp. 8746-8754 ◽  
Author(s):  
Diego J. Díaz ◽  
Stefan Bernhard ◽  
Gregory D. Storrier ◽  
Héctor D. Abruña
Keyword(s):  
Self Assembly ◽  
Ordered Arrays ◽  
Redox Active

scholarly journals Microphase Separation of a PS-b-PFS Block CopolymerviaSolvent Annealing: Effect of Solvent, Substrate, and Exposure Time on Morphology

2015 ◽  
Vol 2015 ◽  
pp. 1-10
Author(s):  
Colm T. O’Mahony ◽  
Dipu Borah ◽  
Michael A. Morris
Keyword(s):  
Block Copolymer ◽  
Self Assembly ◽  
Microphase Separation ◽  
Annealing Effect ◽  
Solvent Annealing ◽  
Spin Casting ◽  
Effect Of Solvent ◽  
Ordered Arrays ◽  
Annealing Conditions ◽  
Nanoscale Features

Block copolymer (BCP) lithography makes use of the microphase separation properties of BCPs to pattern ordered nanoscale features over large areas. This work presents the microphase separation of an asymmetric polystyrene-block-poly(ferrocenyl dimethylsilane) (PS-b-PFS) BCP that allows ordered arrays of nanostructures to be formed by spin casting PS-b-PFS on substrates and subsequent solvent annealing. The effects of the solvent annealing conditions on self-assembly and structural stability are discussed.

scholarly journals Self-assembled peptide nanostructures for electrical, optical, and magnetic applications

2018 ◽  
Author(s):  
◽  
Soma Khanra
Keyword(s):  
Electron Microscopy ◽  
Self Assembly ◽  
Nonlinear Optical ◽  
Electronic Devices ◽  
Longitudinal Component ◽  
The Self ◽  
Assembly Process ◽  
Experimental Characterization ◽  
X Ray ◽  
Self Assembled

Bio-nanotechnology has become a widespread exciting field of research as the basic biological structure of bio-inspired materials and nanotechnology share the common length scale. Bio-nanotechnology, which is mainly based on bio-inspired nanostructured materials, has potential applications in nanomedicine, drug delivery, bio-sensors, and bio-degradable electronic devices. The nanostructures obtained from biomolecules are attractive due to their biocompatibility for molecular recognition, ease of chemical modification, and the ability to scaffold other organic and inorganic materials. Peptide nanostructures formed through the self-assembly process of the basic building block of diphenylalanine show promising applications in biodegradable electronic devices, drug delivery, catalysis agent, waveguide, and frequency converter. This research focusses on the self-assembly process in a dipeptide, L, L diphenylalanine (FF) and exploring its electronic, optical, and magnetic properties. The role of solvents in the self-assembly process of FF is explored by combining density functional theory (DFT) along with experimental characterization techniques such as electron microscopy, Raman scattering, and x-ray diffraction (XRD). One of the objectives of this work was to explore the nonlinear optical (NLO) properties of FF nanostructures via second harmonic generation (SHG). The ratio of the nonlinear optical coefficients was obtained from individual FF nanotubes as a function of the tube diameter and thermal annealing conditions. The ratio of the shear to the longitudinal component (d15/d33) of the NLO coefficient increases with the diameter of the tubes. One of the transverse components, d31, of the NLO coefficient is found to be negative, and its magnitude with respect to the longitudinal component (d33) increases with the tube diameter. Thermal treatment of individual FF tubes has a similar effect as increasing the diameter of the tubes in SHG polarimetry. The functionalization of FF micro-nanostructures (FF-MNS) with nanomaterials was studied. FF-MNS with Ag or Au nanoparticles were explored in surface-enhanced Raman scattering (SERS). Such self-assembled nanostructures provide a natural template for tethering Au and Ag nanoparticles (Nps) due to its fractal surface. The FF-MNS undergo an irreversible phase transition from hexagonal packing (hex) to an orthorhombic (ort) structure at [about] 150 [degree]C. The metal Nps form chains on hex FF-MNS as inferred from transmission electron microscopy images and a uniform non-aggregated distribution in the ort phase. The SERS spectra obtained from R6G bound to FF-MNSs with AuNps show a higher enhancement for the ort phase compared with the hex phase. The experimental results agree well with our calculated Raman spectra of model systems using DFT. Our results indicate that FF-MNS both in the hex and ort phase can be used as substrates for SERS analysis with different metal Nps, opening up a novel class of optically active bio-based substrates. The use of magnetic nanoparticles with biomolecules offers a versatile path for tuning the functionality of the composite material for several applications. The functionalization of FF-MNS with cobalt ferrite (CFO) magnetic nanoparticles was achieved. The interaction between CFO nanoparticles and FF-MNS was investigated by optical spectroscopy, x-ray photoelectron spectroscopy (XPS), and magnetization measurements. The changes in the XPS data from pristine FF-MNS and CFO:FF-MNS are indicative of a charge transfer process from CFO to FF-MNS, changing the electronic states of the Fe2+ and Co2+ ions. A comparison of the magnetic characterization from CFO nanoparticles and CFO:FF-MNS shows a higher saturation magnetization from the nanocomposite sample, which is attributed to a change in the cationic distribution in CFO upon binding with the peptide. We were further successful in demonstrating the application of FF-MNS as a bio-degradable active layer in an organic light emitting diode (OLED). FF-MNS were functionalized with two blue-emitting conducting polymers: di-octyl-substituted polyfluorene (PF8) and ethyl-hexyl polyfluorene (PF2/6), and used as an active layer in an OLED architecture. A combination of molecular dynamics and experimental characterization techniques reveals a stronger binding mechanism for PF8 compared to PF2/6 with FF-MNS. Biodegradability tests from FF-MNS:PF8 nanocomposite films show more than 80% weight loss in 2 h by enzymatic action compared to PF8 pristine films, which do not degrade. Self-assembled FF-MNS with organic semiconductors open up a new generation of biocompatible and biodegradable materials in organic electronics.

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